Visitor Monitoring Drug History: ZEMURON
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Label and Approval History

Drug Name: ZEMURON
FDA Application No: (NDA) 020214
Active Ingredient(s): ROCURONIUM BROMIDE
Company: ORGANON USA INC
 
Label History
 
Labels are not available on this site for ZEMURON, (NDA) 020214
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
8/18/2004 021Labeling Revision Letter 
6/4/2003 017Labeling Revision Letter 
2/6/2004 016Labeling Revision Letter 
7/20/2001 015Control Supplement  
6/5/2001 013Labeling Revision  
3/27/2000 010Labeling Revision  
3/17/1999 009Manufacturing Change or Addition  
3/27/2000 008Labeling Revision  
6/30/1997 007Control Supplement  
12/3/1997 006Control Supplement  
7/25/1996 005Control Supplement  
6/21/1996 004Package Change  
12/7/1994 003Labeling Revision  
10/4/1995 002Control Supplement  
11/22/1994 001Control Supplement  
3/17/1994 000Approval  
 
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